Modified Labeling for Polyderm Wbc(Tm)

FDA 510(k) K890940 · Laivan Corp.

Substantially Equivalent

510(k) numberK890940

Submission

Device name
Modified Labeling for Polyderm Wbc(Tm)
Applicant
Laivan Corp.
East Rockaway, NY, US
Received
February 22, 1989
Decision date
April 17, 1989
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
NAD – Dressing, Wound, Occlusive
Device class
Class I (low risk)
Regulation
21 CFR 878.4020
Specialty
General, Plastic Surgery

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K091133Aplion Topical Care SystemNAD · Traditional Aplion Medical,Llc05/20/2009SE
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K080524Centurion Sorbaview OTCNAD · Traditional Tri-State Hospital Supply Corp.04/23/2008SE
K060046DermastreamNAD · Traditional Enzysurge , Ltd.02/27/2006SE
K043063Oxyband Wound DressingNAD · Traditional Oxyband Technologies, Inc.03/24/2005SE
K020781Wet ChamberNAD · Traditional Kinetic Concepts, Inc.05/06/2002SE
K990530Kerlix MD Antimicrobial Gauze DressingNAD · Traditional The Kendall Company, L.P.01/31/2000SE
K990861Wound Dressing/Abd Pad, Model #10810NAD · Traditional Hospital Specialty Co.04/12/1999SE

More from Hospital Specialty Co.

510(k)DeviceDecision
K923815Total Protective Breatheable Surgical GownsFYA · Traditional 03/31/1993SE
K885205AquadermKGX · Traditional 03/29/1989SN
K880153Polyderm A+B(Tm)NAD · Traditional 04/13/1988SN
K880964Polyderm Pec(Tm), Porous Elastic CoverKGX · Traditional 03/17/1988SN
K880206Polyderm WBC (TM), Waterproof Breathable CoverNAD · Traditional 03/11/1988SN

Questions and answers

When was Modified Labeling for Polyderm Wbc(Tm) cleared by the FDA?

Modified Labeling for Polyderm Wbc(Tm) (K890940) received a 510(k) decision of Substantially Equivalent on April 17, 1989, 54 days after the submission was received.

What is the product code of K890940?

The FDA product code is NAD – Dressing, Wound, Occlusive, a Class I (low risk) device regulated under 21 CFR 878.4020.